Canonical Allele Identifier: CA2156012762

Gene: SERPINA12

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.94497767G= , CM000676.2:g.94497767G=	GRCh38
NC_000014.8:g.94964104G= , CM000676.1:g.94964104G=	GRCh37
NC_000014.7:g.94033857G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001382267.1:c.631C= MANE Select	NP_001369196.1:p.Arg211=
ENST00000677451.1:c.631C= MANE Select	ENSP00000503935.1:p.Arg211=
NM_001304461.1:c.631C=	NP_001291390.1:p.Arg211=
NM_001304461.2:c.631C=	NP_001291390.1:p.Arg211=
NM_173850.3:c.631C=	NP_776249.1:p.Arg211=
NM_173850.4:c.631C=	NP_776249.1:p.Arg211=
ENST00000341228.2:c.631C=	ENSP00000342109.2:p.Arg211=
ENST00000556881.5:c.631C=	ENSP00000451738.1:p.Arg211=
XM_011536451.1:c.631C=	XP_011534753.1:p.Arg211=
XM_011536451.3:c.631C=	XP_011534753.1:p.Arg211=
XM_011536452.1:c.631C=	XP_011534754.1:p.Arg211=
XM_011536452.3:c.631C=	XP_011534754.1:p.Arg211=
XM_011536453.1:c.631C=	XP_011534755.1:p.Arg211=
XM_011536453.2:c.631C=	XP_011534755.1:p.Arg211=
XM_011536454.1:c.631C=	XP_011534756.1:p.Arg211=
XM_011536454.3:c.631C=	XP_011534756.1:p.Arg211=
XM_011536455.1:c.631C=	XP_011534757.1:p.Arg211=
XM_017020989.2:c.631C=	XP_016876478.1:p.Arg211=
XM_017020990.1:c.631C=	XP_016876479.1:p.Arg211=